ClinVar Miner

List of variants in gene TYK2 reported as uncertain significance by Illumina Laboratory Services, Illumina

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Gene type:
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Total variants: 86
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HGVS dbSNP gnomAD frequency
NM_003331.5(TYK2):c.*120C>T rs556369340 0.00159
NM_003331.5(TYK2):c.1869C>T (p.Asp623=) rs140078545 0.00110
NM_003331.5(TYK2):c.2250C>T (p.Gly750=) rs138652649 0.00093
NM_003331.5(TYK2):c.193+14G>A rs199931972 0.00041
NM_003331.5(TYK2):c.2985C>T (p.Ile995=) rs147442318 0.00031
NM_003331.5(TYK2):c.648G>A (p.Pro216=) rs142642403 0.00030
NM_003331.5(TYK2):c.1141C>T (p.Arg381Trp) rs201240289 0.00027
NM_003331.5(TYK2):c.2670G>C (p.Thr890=) rs144332908 0.00026
NM_003331.5(TYK2):c.211T>C (p.Phe71Leu) rs374071090 0.00022
NM_003331.5(TYK2):c.2017G>T (p.Val673Leu) rs528691386 0.00021
NM_003331.5(TYK2):c.1807G>A (p.Val603Met) rs140594440 0.00019
NM_003331.5(TYK2):c.*174G>A rs534835524 0.00016
NM_003331.5(TYK2):c.2102G>C (p.Arg701Thr) rs200791116 0.00014
NM_003331.5(TYK2):c.-145C>T rs778404429 0.00013
NM_003331.5(TYK2):c.630-3C>T rs750663278 0.00013
NM_003331.5(TYK2):c.-322C>T rs548281602 0.00011
NM_003331.5(TYK2):c.-79C>G rs921883780 0.00011
NM_003331.5(TYK2):c.589C>T (p.Arg197Cys) rs376427383 0.00011
NM_003331.5(TYK2):c.1559G>A (p.Gly520Asp) rs142576987 0.00010
NM_003331.5(TYK2):c.1806C>T (p.Asn602=) rs765576893 0.00010
NM_003331.5(TYK2):c.1398C>T (p.Pro466=) rs200752112 0.00009
NM_003331.5(TYK2):c.2441C>T (p.Pro814Leu) rs143743593 0.00009
NM_003331.5(TYK2):c.727C>T (p.Arg243Trp) rs200003143 0.00009
NM_003331.5(TYK2):c.1342C>T (p.Arg448Trp) rs147991080 0.00008
NM_003331.5(TYK2):c.3560G>A (p.Cys1187Tyr) rs200932305 0.00008
NM_003331.5(TYK2):c.372T>C (p.Arg124=) rs371832787 0.00008
NM_003331.5(TYK2):c.489C>T (p.Asp163=) rs748475805 0.00008
NM_003331.5(TYK2):c.783C>G (p.Ala261=) rs371939297 0.00008
NM_003331.5(TYK2):c.2176-9C>T rs370673325 0.00006
NM_003331.5(TYK2):c.329G>A (p.Arg110Gln) rs56090991 0.00006
NM_003331.5(TYK2):c.493G>A (p.Ala165Thr) rs370420133 0.00006
NM_003331.5(TYK2):c.*173C>T rs766203641 0.00005
NM_003331.5(TYK2):c.-37C>T rs1166754820 0.00005
NM_003331.5(TYK2):c.1851G>A (p.Glu617=) rs780346579 0.00005
NM_003331.5(TYK2):c.2038G>A (p.Gly680Ser) rs745582179 0.00005
NM_003331.5(TYK2):c.2687A>G (p.Tyr896Cys) rs372017111 0.00005
NM_003331.5(TYK2):c.3487G>A (p.Glu1163Lys) rs529855217 0.00005
NM_003331.4(TYK2):c.*302C>T rs886054131 0.00004
NM_003331.5(TYK2):c.1254G>A (p.Ser418=) rs201945206 0.00004
NM_003331.5(TYK2):c.1469G>A (p.Arg490His) rs369615833 0.00004
NM_003331.5(TYK2):c.1839C>T (p.Ser613=) rs748006603 0.00004
NM_003331.5(TYK2):c.1968C>T (p.Tyr656=) rs764154157 0.00004
NM_003331.5(TYK2):c.3239A>G (p.Tyr1080Cys) rs776034616 0.00004
NM_003331.5(TYK2):c.*260C>T rs1258476690 0.00003
NM_003331.5(TYK2):c.1576G>A (p.Val526Ile) rs758682935 0.00003
NM_003331.5(TYK2):c.2646G>C (p.Pro882=) rs184567726 0.00003
NM_003331.5(TYK2):c.505G>A (p.Glu169Lys) rs778545468 0.00003
NM_003331.5(TYK2):c.670C>T (p.Arg224Trp) rs920085264 0.00003
NM_003331.5(TYK2):c.2197G>A (p.Gly733Ser) rs1038590632 0.00002
NM_003331.5(TYK2):c.2370C>T (p.Ser790=) rs762732975 0.00002
NM_003331.5(TYK2):c.3201-15C>T rs766488790 0.00002
NM_003331.5(TYK2):c.3555C>T (p.Ser1185=) rs372903125 0.00002
NM_003331.5(TYK2):c.*291T>C rs537387706 0.00001
NM_003331.5(TYK2):c.1444C>T (p.Arg482Cys) rs146770568 0.00001
NM_003331.5(TYK2):c.2124G>A (p.Met708Ile) rs201502911 0.00001
NM_003331.5(TYK2):c.2658G>A (p.Ala886=) rs761205319 0.00001
NM_003331.5(TYK2):c.328C>T (p.Arg110Trp) rs747918278 0.00001
NM_003331.5(TYK2):c.3525G>A (p.Lys1175=) rs377283866 0.00001
NM_003331.5(TYK2):c.370C>T (p.Arg124Cys) rs757581005 0.00001
NM_003331.5(TYK2):c.602C>T (p.Pro201Leu) rs752615354 0.00001
NM_003331.5(TYK2):c.661C>T (p.Arg221Trp) rs200858844 0.00001
NM_003331.5(TYK2):c.829G>A (p.Val277Met) rs148520054 0.00001
NM_003331.5(TYK2):c.879C>T (p.Ile293=) rs375414145 0.00001
NM_003331.5(TYK2):c.*261C>A rs1313565853
NM_003331.5(TYK2):c.*63G>A rs185435731
NM_003331.5(TYK2):c.-154A>G rs2042302135
NM_003331.5(TYK2):c.-23C>T rs886054135
NM_003331.5(TYK2):c.-328T>G rs886054136
NM_003331.5(TYK2):c.-369C>T rs886054137
NM_003331.5(TYK2):c.-9G>A rs2042248932
NM_003331.5(TYK2):c.1000A>G (p.Asn334Asp) rs886054133
NM_003331.5(TYK2):c.1011+12G>A rs377517686
NM_003331.5(TYK2):c.124C>A (p.Pro42Thr) rs147251502
NM_003331.5(TYK2):c.1489A>C (p.Met497Leu) rs751952281
NM_003331.5(TYK2):c.1669+12G>A rs2041444641
NM_003331.5(TYK2):c.2023G>A (p.Gly675Ser) rs2041401700
NM_003331.5(TYK2):c.2036G>C (p.Arg679Pro) rs200247986
NM_003331.5(TYK2):c.2558C>G (p.Pro853Arg) rs551747806
NM_003331.5(TYK2):c.2618-14C>G rs532521303
NM_003331.5(TYK2):c.2715+9C>T rs886054132
NM_003331.5(TYK2):c.2716-13C>A rs370899700
NM_003331.5(TYK2):c.3200+11G>A rs2040885202
NM_003331.5(TYK2):c.3236A>G (p.Tyr1079Cys) rs2040862596
NM_003331.5(TYK2):c.498A>G (p.Ser166=) rs969593614
NM_003331.5(TYK2):c.737A>G (p.Gln246Arg) rs886054134
NM_003331.5(TYK2):c.975G>T (p.Gln325His) rs762767796

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